FDA Warning Letter — Ulrich Gmbh & Co. KG

Case 407860 — FEI 3002807156

The FDA took a Warning Letter action against Ulrich Gmbh & Co. KG on Aug 15, 2013 (Ulm, Germany). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action details

Facility
Ulrich Gmbh & Co. KG
Date
Aug 15, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Ulm (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.